Northeastern University Biologist Finds Link Between “Bloodless” Icefish of Antarctica and Anemia and Osteoporosis
Researchers receive $2.48 million grant from NIH
New research by Northeastern University Professor William Detrich argues that Antarctic icefish are "evolutionary mutant models" that hold important clues for understanding, and eventually treating, human diseases including osteoporosis and anemia. The success of the project studying the mineralization of the icefish skeleton as a model for osteopenia (low bone density) and osteoporosis (the disease that results from osteopenia) prompted the National Institutes of Health to fund further studies with a $2.48 million grant.
The innovative approach by Dr. William Detrich, professor of biochemistry and marine biology at Northeastern University and colleagues from other universities to learning how the regulation of bone calcification can lead to osteoporosis in the elderly is discussed in the latest issue of Trends in Genetics. The researchers will build upon these findings over the next 5 years as part of the grant.
“There is a growing recognition among biologists that organisms that live in novel environments have evolved certain characteristics that work well for them but would cause disease in humans,” said Detrich. “There is a lot that evolution and adaptation can tell us about the human condition. Oddball creatures, such as cavefish that lack eyes, giraffes with high blood pressure, and Antarctic fishes, provide powerful research systems that complement the more traditional models of human disease, like the mouse.”
Through the replacement of bone by connective tissue and decreased mineralization of the skeleton as a whole, many Antarctic fish species have evolved reduced bone density. This adaptation increases their buoyancy in water, a characteristic that enables them to move easily in the water column for feeding. This adaptive trait clearly mimics the detrimental human condition osteopenia, a reduction in bone mineral density that affects 34 million American women and 12 million American men.
Osteopenia can lead to osteoporosis, a disease characterized by low bone mass, bone deterioration and fragility, and increased susceptibility to and slow healing of fractured bones. The authors propose that the type and mode of action of adaptive mutations favored by natural selection in wild populations—such as low bone density for increased buoyancy in Antarctic fishes—are similar to those that contribute to human diseases like osteoporosis. Studies in evolutionary mutant models have the potential to identify presently unknown genes and gene/environment interactions that affect human health and underlie human disease.
A subset of Antarctic fishes, the icefishes, too, have acquired the characteristics of human disease. Icefishes do not make hemoglobin, the oxygen-transporting protein of all other vertebrates, or produce red blood cells: they are profoundly anemic. Nevertheless, icefishes survive and thrive in oxygen-rich cold waters surrounding Antarctica. In humans, anemia (reduced numbers of circulating red blood cells) is deleterious because it greatly reduces delivery of oxygen to the body tissues. Patients undergoing kidney dialysis or chemotherapy often suffer from anemia.
Work from Detrich’s laboratory on the icefishes has already revealed novel genes involved in red cell formation that might be developed as new targets for anemia treatments, providing further support for the potential large role that studies of evolutionary mutant models can play in improving human health.
For more information please contact Samantha Fodrowski at 617-373-5427 or email@example.com.
Photo of the icefish Chionodraco hamatus by H. William Detrich.
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